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NCT05731284 · ClinicalTrials.gov registry record · NA

Platelet Rich Plasma as an Adjunct Therapy at the Time of Transvaginal Native Tissue Prolapse Surgery

A NA study of Pelvic Organ Prolapse, sponsored by University of Alabama at Birmingham.

Active
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT05731284 is a NA study of Pelvic Organ Prolapse that is active but no longer recruiting, run by University of Alabama at Birmingham. The registered enrollment target is 60 participants, below the 144-participant average among 40 other Pelvic Organ Prolapse trials with a reported enrollment target (58% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05731284, a NA study of Pelvic Organ Prolapse, is active but no longer recruiting, sponsored by University of Alabama at Birmingham.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

The purpose of the study is to evaluate the surgical outcomes of injecting platelet-rich plasma (PRP) into the vaginal tissue as an adjunct therapy at the time of prolapse surgery

Conditions Studied

Interventions

  • PROCEDURE Placebo
  • PROCEDURE Platelet rich plasma (PRP) Injection

Study Locations (1)

Alabama

  • University of Alabama at Birmingham - Birmingham

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2023-07-01
Est. Completion 2028-12-31
Phase NA

Sponsor

University of Alabama at Birmingham

1,160 total trials

What the Registry Record Tells You About NCT05731284

The ClinicalTrials.gov registry entry for NCT05731284 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 144-participant average among 40 other Pelvic Organ Prolapse trials with a reported enrollment target (58% lower). The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pelvic Organ Prolapse appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT05731284 reports 1 study location spanning 1 distinct geographic area - top geographies include Alabama.

Frequently Asked Questions

What is clinical trial NCT05731284 about?

NCT05731284 is a clinical study titled "Platelet Rich Plasma as an Adjunct Therapy at the Time of Transvaginal Native Tissue Prolapse Surgery". The purpose of the study is to evaluate the surgical outcomes of injecting platelet-rich plasma (PRP) into the vaginal tissue as an adjunct therapy at the time of prolapse surgery

What is the current status of trial NCT05731284?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2023-07-01. Estimated completion is 2028-12-31.

What conditions does trial NCT05731284 study?

This clinical trial studies the following conditions: Pelvic Organ Prolapse.

What interventions are being tested in trial NCT05731284?

The interventions under investigation include: Placebo (PROCEDURE), Platelet rich plasma (PRP) Injection (PROCEDURE).

Who is sponsoring clinical trial NCT05731284?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05731284 being conducted?

This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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